Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype.
Saved in:
| Title: | Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype. |
|---|---|
| Authors: | Sharma, Prashant1,2 sharmap@mail.nih.gov, Reichert, Marie1,2, Lu, Yan3, Markello, Thomas C.1,2,4, Adams, David R.1,2, Steinbach, Peter J.5, Fuqua, Brie K.6, Parisi, Xenia1,2, Kaler, Stephen G.7, Vulpe, Christopher D.8, Anderson, Gregory J.3, Gahl, William A.1,2,4, Malicdan, May Christine V.1,2 |
| Source: | PLoS Genetics. 5/24/2019, Vol. 15 Issue 5, p1-24. 24p. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
Be the first to leave a comment!